The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
77984279 7798427 9 F 20101215 20160824 20110203 20160901 EXP US-ASTRAZENECA-2011SE04545 ASTRAZENECA 28113.00 DY F Y 89.10000 KG 20160901 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
77984279 7798427 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 8940 MG Y U 21153 20 MG QD
77984279 7798427 2 SS NAPROXEN. NAPROXEN 1 Oral TWICE A DAY. Y U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77984279 7798427 1 Gastritis prophylaxis
77984279 7798427 2 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
77984279 7798427 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
77984279 7798427 Anaemia
77984279 7798427 Constipation
77984279 7798427 Dehydration
77984279 7798427 Diverticulitis intestinal haemorrhagic
77984279 7798427 Large intestinal ulcer
77984279 7798427 Nausea
77984279 7798427 Spinal compression fracture
77984279 7798427 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
77984279 7798427 1 20090925 20101215 0
77984279 7798427 2 20090926 20101215 0